Univariate analyses of potential viables for survival of patients with HCC
Variables
OS
RFS
DR (95% CI)
Ptrend
TRR (95% CI)
Ptrend
Age (> 48 years old vs. 48 years old)a
0.89 (0.70–1.12)
0.31
0.88 (0.69–1.12)
0.29
Gender (female vs. male)
0.91 (0.71–1.17)
0.47
0.90 (0.70–1.15)
0.39
Ethnicity (Zhuang vs. Han)
0.81 (0.64–1.02)
0.07
0.77 (0.61–1.08)
0.08
Smoking (yes vs. no)
0.76 (0.58–0.99)
0.05
0.76 (0.58–1.01)
0.06
Drinking (yes vs. no)
0.86 (0.66–1.12)
0.26
0.82 (0.63–1.08)
0.16
HBV status (positive vs. negative)
1.04 (0.81–1.33)
0.79
1.20 (0.93–1.55)
0.16
HCV status (positive vs. negative)
1.03 (0.72–1.48)
0.86
1.03 (0.71–1.50)
0.87
AFP (> 20 ng/mL vs. 20 ng/mL)
1.11 (0.88–1.41)
0.38
1.21 (0.95–1.55)
0.13
Liver cirrhosis (yes vs. no)
1.20 (0.92–1.58)
0.19
1.13 (0.85–1.49)
0.40
ES grade (high vs. low)
1.48 (1.17–1.87)
8.99 10–4
1.57 (1.24–1.99)
2.11 × 10–4
MVD (positive vs. negative)
1.39 (1.09–1.78)
7.30 10–5
1.22 (0.96–1.57)
0.11
Po-TACE treatment (yes vs. no)
0.63 (0.50–0.80)
9.80 10–5
0.61 (0.48–0.78)
5.10 × 10–5
ADAs (high vs. low)b
3.89 (2.95–5.12)
4.66 10–22
3.08 (2.36–4.02)
1.10 × 10–16
a Age is grouped according to the average age of patients with HCC (47.94 years old 9.98 years old); b ADAs are grouped according to the average ADA of patients with HCC (3.00 µmol/mol 1.51 µmol/mol DNA). Ptrend: P value is calculated by trend test in the models
Declarations
Acknowledgement
We thank Dr. Qiu-Xiang Liang, Dr. Yun Yi, Yun Xia, Yong-Zhi Huang, and Dr. Yuan-Feng Zhou for sample collection and management, Dr. Hua Huang for molecular biochemical technique.
Author contributions
LYH and QQL: Methodology, Formal analysis, Data curation, Writing—review & editing. QYS: Investigation, Resource, Writing—review & editing. XYZ: Investigation, Formal analysis, Writing—review & editing. XDL: Conceptualization, Funding acquisition, Supervision, Project administration, Writing—original draft, Writing—review & editing. All authors read and approved the submitted version.
Conflicts of interest
The authors declare that they have no conflicts of interest.
Ethical approval
The collection of removed tumor samples and clinicopathological information are approved by the Ethics Committee of Youjiang Medical University for Nationalities, China (No. AYJM20150118) and comply with the Declaration of Helsinki.
Consent to participate
Informed consent to participate in the study was obtained from all participants.
Consent to publication
Not applicable.
Availability of data and materials
Not applicable.
Funding
This study was supported in part by Guangxi Training Program for Medical High-level Academic Leaders [Guiweikejiaofa (2020)-15], Bose Talent Highland [2020-3-2], Building Projects from the Key Laboratory of Molecular Pathology (Hepatobiliary Diseases) of Guangxi [Guiweikejiaofa (2020)-17] and the Key Laboratory of Tumor Molecular Pathology of Guangxi Colleges & Universities [Guijiaokeyan (2022)-10], and Clinical Key Specialty Building Project (For Pathology) of Guangxi [Guiweiyifa (2022)-21]. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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